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Survivin expression in oral lichen planus: Role in malignant transformation
CONTEXT: Oral lichen planus (OLP) is a potentially malignant disease with a prevalence rate of 0.5–2.2%. It is a T-cell-mediated autoimmune disease, in which cytotoxic CD8+ T-cells trigger apoptosis of the basal cells of oral epithelium. The reported progression of OLP to oral squamous cell carcinom...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4989553/ https://www.ncbi.nlm.nih.gov/pubmed/27601815 http://dx.doi.org/10.4103/0973-029X.185912 |
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author | Suganya, G Bavle, Radhika M Paremala, K Makarla, Soumya Sudhakar, M Reshma, V |
author_facet | Suganya, G Bavle, Radhika M Paremala, K Makarla, Soumya Sudhakar, M Reshma, V |
author_sort | Suganya, G |
collection | PubMed |
description | CONTEXT: Oral lichen planus (OLP) is a potentially malignant disease with a prevalence rate of 0.5–2.2%. It is a T-cell-mediated autoimmune disease, in which cytotoxic CD8+ T-cells trigger apoptosis of the basal cells of oral epithelium. The reported progression of OLP to oral squamous cell carcinoma (OSCC) ranges from 0.4% to 6.5%. Apoptosis plays a major role in the maintenance of tissue homeostasis. The evasion of apoptosis in the form of dysregulation of inhibitors of apoptosis proteins (IAPs) may lead to malignant transformation. Survivin belongs to the second gene family of IAPs, which is overexpressed in many tumors such as OSCC and gastric carcinomas, and its expression is widely involved in apoptosis as well as in tumor metastasis. MATERIALS AND METHODS: Sections were obtained from the paraffin-embedded archival blocks of patients diagnosed histologically as OLP, and cases with normal epithelium were used for comparison whereas cases with OSCC were used as positive control. RESULTS: We analyzed the expression of survivin in OLP and normal epithelium. Survivin expression with moderate intensity was seen in the cells of basal layer with nuclear positivity in cases of OLP, whereas mild to nil expression was seen in normal epithelium with nuclear and cytoplasmic positivity in different layers. CONCLUSIONS: Survivin positivity was seen predominantly in the basal cells of OLP suggesting increased longevity of these cells which in turn might acquire dysplastic changes leading to increased risk of malignant transformation of this premalignant condition. Although the conversion rate may be low, the potential exists in the indolent course of the disease. |
format | Online Article Text |
id | pubmed-4989553 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-49895532016-09-06 Survivin expression in oral lichen planus: Role in malignant transformation Suganya, G Bavle, Radhika M Paremala, K Makarla, Soumya Sudhakar, M Reshma, V J Oral Maxillofac Pathol Original Article CONTEXT: Oral lichen planus (OLP) is a potentially malignant disease with a prevalence rate of 0.5–2.2%. It is a T-cell-mediated autoimmune disease, in which cytotoxic CD8+ T-cells trigger apoptosis of the basal cells of oral epithelium. The reported progression of OLP to oral squamous cell carcinoma (OSCC) ranges from 0.4% to 6.5%. Apoptosis plays a major role in the maintenance of tissue homeostasis. The evasion of apoptosis in the form of dysregulation of inhibitors of apoptosis proteins (IAPs) may lead to malignant transformation. Survivin belongs to the second gene family of IAPs, which is overexpressed in many tumors such as OSCC and gastric carcinomas, and its expression is widely involved in apoptosis as well as in tumor metastasis. MATERIALS AND METHODS: Sections were obtained from the paraffin-embedded archival blocks of patients diagnosed histologically as OLP, and cases with normal epithelium were used for comparison whereas cases with OSCC were used as positive control. RESULTS: We analyzed the expression of survivin in OLP and normal epithelium. Survivin expression with moderate intensity was seen in the cells of basal layer with nuclear positivity in cases of OLP, whereas mild to nil expression was seen in normal epithelium with nuclear and cytoplasmic positivity in different layers. CONCLUSIONS: Survivin positivity was seen predominantly in the basal cells of OLP suggesting increased longevity of these cells which in turn might acquire dysplastic changes leading to increased risk of malignant transformation of this premalignant condition. Although the conversion rate may be low, the potential exists in the indolent course of the disease. Medknow Publications & Media Pvt Ltd 2016 /pmc/articles/PMC4989553/ /pubmed/27601815 http://dx.doi.org/10.4103/0973-029X.185912 Text en Copyright: © 2016 Journal of Oral and Maxillofacial Pathology http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms. |
spellingShingle | Original Article Suganya, G Bavle, Radhika M Paremala, K Makarla, Soumya Sudhakar, M Reshma, V Survivin expression in oral lichen planus: Role in malignant transformation |
title | Survivin expression in oral lichen planus: Role in malignant transformation |
title_full | Survivin expression in oral lichen planus: Role in malignant transformation |
title_fullStr | Survivin expression in oral lichen planus: Role in malignant transformation |
title_full_unstemmed | Survivin expression in oral lichen planus: Role in malignant transformation |
title_short | Survivin expression in oral lichen planus: Role in malignant transformation |
title_sort | survivin expression in oral lichen planus: role in malignant transformation |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4989553/ https://www.ncbi.nlm.nih.gov/pubmed/27601815 http://dx.doi.org/10.4103/0973-029X.185912 |
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